rs398122562

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;TA)	6	BRCA2 variant considered pathogenic for breast cancer

Make rs398122562(TA;TA)

Reference

GRCh38 38.1/141

Chromosome

13

Position

32340982

Gene

BRCA2

is a	snp
is	mentioned by
dbSNP	rs398122562
dbSNP (classic)	rs398122562
ClinGen	rs398122562
ebi	rs398122562
HLI	rs398122562
Exac	rs398122562
Gnomad	rs398122562
Varsome	rs398122562
LitVar	rs398122562
Map	rs398122562
PheGenI	rs398122562
Biobank	rs398122562
1000 genomes	rs398122562
hgdp	rs398122562
ensembl	rs398122562
geneview	rs398122562
scholar	rs398122562
google	rs398122562
pharmgkb	rs398122562
gwascentral	rs398122562
openSNP	rs398122562
23andMe	rs398122562
SNPshot	rs398122562
SNPdbe	rs398122562
MSV3d	rs398122562
GWAS Ctlg	rs398122562

Max Magnitude

6

ClinVar
Risk	rs398122562(AT;AT)
Alt	rs398122562(AT;AT)
Reference	Rs398122562(-;-)
Significance	Pathogenic
Disease	Breast-ovarian cancer
Variation	info
Gene	BRCA2
CLNDBN	Breast-ovarian cancer, familial 2
Reversed	0
HGVS	NC_000013.10:g.32915118_32915119dupTA
CLNSRC	ClinVar
CLNACC	RCV000076971.4,